JP3917863B2 - Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 - Google Patents
Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 Download PDFInfo
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- JP3917863B2 JP3917863B2 JP2001557868A JP2001557868A JP3917863B2 JP 3917863 B2 JP3917863 B2 JP 3917863B2 JP 2001557868 A JP2001557868 A JP 2001557868A JP 2001557868 A JP2001557868 A JP 2001557868A JP 3917863 B2 JP3917863 B2 JP 3917863B2
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- Prior art keywords
- formula
- methyl
- nicotinamide
- benzo
- oxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- YLVAGBJBSYSJJJ-UHFFFAOYSA-N CC(C(C(c(cc1)ccc1SC)=O)N1)NC1=O Chemical compound CC(C(C(c(cc1)ccc1SC)=O)N1)NC1=O YLVAGBJBSYSJJJ-UHFFFAOYSA-N 0.000 description 1
- GRNSAEXUTAGBSL-UHFFFAOYSA-N CC(C)(c1ccc(CN(CC=C)CC=C)cc1)O Chemical compound CC(C)(c1ccc(CN(CC=C)CC=C)cc1)O GRNSAEXUTAGBSL-UHFFFAOYSA-N 0.000 description 1
- NDHOQAPKKVXVEH-UHFFFAOYSA-N CC(C)C(C(C)C)C(c(cc1OC)ccc1OCCCCCOc(cc1)ccc1C(N)=N)=O Chemical compound CC(C)C(C(C)C)C(c(cc1OC)ccc1OCCCCCOc(cc1)ccc1C(N)=N)=O NDHOQAPKKVXVEH-UHFFFAOYSA-N 0.000 description 1
- NPFVRBCDMFKOPY-UHFFFAOYSA-N CC(C1)C(c2cc(-[n]3cncc3)c[s]2)=NNC1=O Chemical compound CC(C1)C(c2cc(-[n]3cncc3)c[s]2)=NNC1=O NPFVRBCDMFKOPY-UHFFFAOYSA-N 0.000 description 1
- BEIZIEZPGSIQGR-UHFFFAOYSA-N CS(Nc1ccc(Oc(cc2)ccc2F)[s]1)(=O)=O Chemical compound CS(Nc1ccc(Oc(cc2)ccc2F)[s]1)(=O)=O BEIZIEZPGSIQGR-UHFFFAOYSA-N 0.000 description 1
- YEEZWCHGZNKEEK-UHFFFAOYSA-N Cc(cccc1)c1S(NC(c1cc(OC)c(Cc(c2c3)c[n](C)c2ccc3NC(OC2CCCC2)=O)cc1)=O)(=O)=O Chemical compound Cc(cccc1)c1S(NC(c1cc(OC)c(Cc(c2c3)c[n](C)c2ccc3NC(OC2CCCC2)=O)cc1)=O)(=O)=O YEEZWCHGZNKEEK-UHFFFAOYSA-N 0.000 description 1
- ZGSYVUBKPBUTDW-UHFFFAOYSA-N NCc1ccc(C2(CC2)O)cc1 Chemical compound NCc1ccc(C2(CC2)O)cc1 ZGSYVUBKPBUTDW-UHFFFAOYSA-N 0.000 description 1
- DABPGEIBZBRJFL-UHFFFAOYSA-N OC(c(cccn1)c1Oc1cc2n[s]nc2cc1)=O Chemical compound OC(c(cccn1)c1Oc1cc2n[s]nc2cc1)=O DABPGEIBZBRJFL-UHFFFAOYSA-N 0.000 description 1
- 0 [*+]c1ccc(*)[s]1 Chemical compound [*+]c1ccc(*)[s]1 0.000 description 1
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Veterinary Medicine (AREA)
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- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- General Chemical & Material Sciences (AREA)
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- Neurology (AREA)
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- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
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- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Psychology (AREA)
- Endocrinology (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17928400P | 2000-01-31 | 2000-01-31 | |
| US60/179,284 | 2000-01-31 | ||
| PCT/IB2001/000124 WO2001057036A1 (fr) | 2000-01-31 | 2001-01-30 | Derives benzocondenses heterocycliques de nicotinamide utiles comme inhibiteurs selectifs d'isozymes pde4 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003522176A JP2003522176A (ja) | 2003-07-22 |
| JP3917863B2 true JP3917863B2 (ja) | 2007-05-23 |
Family
ID=22655931
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001557868A Expired - Fee Related JP3917863B2 (ja) | 2000-01-31 | 2001-01-30 | Pde4アイソザイムの選択的阻害薬として有用なニコチンアミドベンゾ縮合複素環誘導体 |
Country Status (41)
| Country | Link |
|---|---|
| US (1) | US7354941B2 (fr) |
| EP (1) | EP1252158B1 (fr) |
| JP (1) | JP3917863B2 (fr) |
| KR (1) | KR20020072299A (fr) |
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| DE (1) | DE60110205T2 (fr) |
| EA (1) | EA004885B1 (fr) |
| EE (1) | EE200200425A (fr) |
| ES (1) | ES2238415T3 (fr) |
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| HN (1) | HN2001000019A (fr) |
| HU (1) | HUP0204262A2 (fr) |
| IL (1) | IL150641A0 (fr) |
| IS (1) | IS6421A (fr) |
| MA (1) | MA26870A1 (fr) |
| MX (1) | MXPA02007419A (fr) |
| NO (1) | NO20023613L (fr) |
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| PA (1) | PA8511201A1 (fr) |
| PE (1) | PE20011058A1 (fr) |
| PL (1) | PL357995A1 (fr) |
| PT (1) | PT1252158E (fr) |
| PY (1) | PY0102109A (fr) |
| SK (1) | SK10142002A3 (fr) |
| SV (1) | SV2002000299A (fr) |
| TN (1) | TNSN01020A1 (fr) |
| TR (1) | TR200201880T2 (fr) |
| UY (1) | UY26569A1 (fr) |
| WO (1) | WO2001057036A1 (fr) |
| ZA (1) | ZA200206033B (fr) |
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| ATE457169T1 (de) * | 1998-10-15 | 2010-02-15 | Imp Innovations Ltd | Verbindungen für die behandlung von gewichtsverlust |
| KR100782891B1 (ko) * | 2000-01-28 | 2007-12-06 | 알자 코포레이션 | 과포화 용액으로 포획된 화합물을 포함하는 리포좀 |
| RU2003110962A (ru) * | 2000-09-18 | 2004-10-20 | Е.И.Дюпон де Немур энд Компани (US) | Пиридиниламиды и имиды для использования в качестве фунгицидов |
| KR20030070150A (ko) * | 2001-01-31 | 2003-08-27 | 화이자 프로덕츠 인크. | Pde4 이소자임 억제제로서 유용한 에테르 유도체 |
| OA12542A (en) | 2001-01-31 | 2006-06-05 | Pfizer Prod Inc | Thiazolyl-, oxazolyl-, pyrrolyl-, and imidazolyl-acid amide derivatives useful as inhibitors of PDE4isozymes. |
| US7250518B2 (en) | 2001-01-31 | 2007-07-31 | Pfizer Inc. | Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes |
| JP2004520386A (ja) * | 2001-01-31 | 2004-07-08 | ファイザー・プロダクツ・インク | Pde4アイソザイムの阻害剤として有用なニコチンアミドビアリール誘導体 |
| GB0118373D0 (en) * | 2001-07-27 | 2001-09-19 | Glaxo Group Ltd | Novel therapeutic method |
| US20050014762A1 (en) * | 2001-09-19 | 2005-01-20 | Rolf Beume | Combination |
| MXPA04002562A (es) * | 2001-09-19 | 2004-05-31 | Altana Pharma Ag | Combinacion de un pde-4 y nsaid. |
| IS7221A (is) * | 2001-11-15 | 2004-04-15 | Memory Pharmaceuticals Corporation | Hringlaga adenosínmónófosfat fosfódíesterasa 4D7 ísóform og aðferðir til notkunar þeirra |
| PL372756A1 (en) | 2002-02-11 | 2005-08-08 | Pfizer Inc. | Nicotinamide derivatives useful as pde4 inhibitors |
| US6756392B2 (en) | 2002-02-11 | 2004-06-29 | Pfizer Inc | Nicotinamide derivatives useful as PDE4 inhibitors |
| US6962940B2 (en) | 2002-03-20 | 2005-11-08 | Celgene Corporation | (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione: methods of using and compositions thereof |
| CA2506949A1 (fr) * | 2002-11-27 | 2004-06-10 | Altana Pharma Ag | Inhibiteurs de pde4 et pde3/4 que l'on utilise dans le traitement de la cachexie |
| US20040225077A1 (en) | 2002-12-30 | 2004-11-11 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
| JPWO2004087151A1 (ja) * | 2003-03-31 | 2006-06-29 | 協和醗酵工業株式会社 | 医薬組成物 |
| WO2004087150A1 (fr) * | 2003-03-31 | 2004-10-14 | Kyowa Hakko Kogyo Co. Ltd. | Composition pour medicaments |
| WO2004087149A1 (fr) * | 2003-03-31 | 2004-10-14 | Kyowa Hakko Kogyo Co. Ltd. | Composition therapeutique |
| WO2004090157A1 (fr) * | 2003-04-10 | 2004-10-21 | F. Hoffmann-La Roche Ag | Utilisation de pde4d dans le criblage de medicaments contre l'atherosclerose |
| US20040265323A1 (en) * | 2003-05-16 | 2004-12-30 | Mccormick Beth A. | Compositions comprising pathogen elicited epithelial chemoattractant (eicosanoid hepoxilin A3), inhibitors thereof and methods of use thereof |
| GB0317484D0 (en) | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Nicotinamide derivatives useful as pde4 inhibitors |
| US7132435B2 (en) | 2003-07-25 | 2006-11-07 | Pfizer Inc. | Compounds |
| GB0317498D0 (en) * | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Compounds |
| US7153870B2 (en) | 2003-07-25 | 2006-12-26 | Pfizer Inc. | Nicotinamide derivatives useful as PDE4 inhibitors |
| GB0317471D0 (en) * | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Novel compounds |
| GB0317516D0 (en) | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Nicotinamide derivatives useful as PDE4 inhibitors |
| PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
| EP1683795A1 (fr) * | 2005-01-21 | 2006-07-26 | Pfizer Limited | Formes crystallines de cis-5-fluoro-N-¬4-(2-hydroxy-4-methylbenzamido)cyclohexyl|-2-(tetrahydrothiopyran-4-yloxy)nicotinamide |
| EP1844040A1 (fr) * | 2005-01-21 | 2007-10-17 | Pfizer Limited | Formes crystallines de cis-5-fluoro-n-[4-(2-hydroxy-4-methylbenzamido)cyclohexyl]-2-(tetrahydrothiopyran-4-yloxy)nicotinamide |
| GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| GB0624282D0 (en) * | 2006-12-05 | 2007-01-10 | Cavalla David | Treatment of cachexia |
| WO2008079328A2 (fr) * | 2006-12-22 | 2008-07-03 | Creighton University | Acides gras oméga-5 utiles dans l'inhibition de la 5-lipoxygénase et dans le traitement du cancer |
| RU2009141592A (ru) * | 2007-04-11 | 2011-05-20 | Алькон Рисерч, Лтд. (Us) | ПРИМЕНЕНИЕ ИНГИБИТОРА TNFα В СОЧЕТАНИИ С АНТИГИСТАМИННЫМ СРЕДСТВОМ ДЛЯ ЛЕЧЕНИЯ АЛЛЕРГИЧЕСКОГО РИНИТА И АЛЛЕРГИЧЕСКОГО КОНЪЮНКТИВИТА |
| EP2196465A1 (fr) | 2008-12-15 | 2010-06-16 | Almirall, S.A. | Dérivés de (3-oxo)pyridazin-4-ylurée comme inhibiteurs de PDE4 |
| EP2226323A1 (fr) | 2009-02-27 | 2010-09-08 | Almirall, S.A. | Nouveaux dérivés de tétrahydropyrazolo [3,4-c]isoquinoléine-5-amine |
| RU2569063C2 (ru) | 2009-09-01 | 2015-11-20 | Катабэйсис Фармасьютикалз, Инк. | Конъюгаты жирных кислот и ниацина и их применение |
| USRE46608E1 (en) | 2009-09-01 | 2017-11-14 | Catabasis Pharmaceuticals, Inc. | Fatty acid niacin conjugates and their uses |
| EP2380890A1 (fr) | 2010-04-23 | 2011-10-26 | Almirall, S.A. | Nouveaux dérivés de 7,8-dihydro-1,6-naphthyridin-5(6h)-one comme PDE4 inhibiteurs |
| EP2386555A1 (fr) * | 2010-05-13 | 2011-11-16 | Almirall, S.A. | Nouveaux dérivés de cyclohéxylamine dotés d'activités agoniste bêta 2 adrénergique et antagoniste muscarinique m3 |
| EP2394998A1 (fr) | 2010-05-31 | 2011-12-14 | Almirall, S.A. | Dérivés de 3-(5-Amino-6-oxo-1,6-dihydropyridazin-3-yl)-biphenyl en tant qu'inhibiteurs de la PDE4 |
| EP3270929B1 (fr) * | 2015-03-17 | 2019-09-11 | Lee, Sheau-Long | Utilisation de ginsenoside m1 pour la prévention ou le traitement de la silicose |
| US11116737B1 (en) | 2020-04-10 | 2021-09-14 | University Of Georgia Research Foundation, Inc. | Methods of using probenecid for treatment of coronavirus infections |
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| US4861891A (en) * | 1988-08-31 | 1989-08-29 | Pfizer Inc. | Antidepressant N-substituted nicotinamide compounds |
| TW429148B (en) | 1995-10-27 | 2001-04-11 | Pfizer | Pharmaceutical agents for the treatment of acute and chronic inflammatory diseases |
| SK132899A3 (en) * | 1997-04-04 | 2000-09-12 | Pfizer Prod Inc | NICOTINAMIDE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONì (54) COMPRISING THEM |
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